Canonical Allele Identifier: PA645406708
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374886
ClinVar RCV Id: RCV000415542 RCV002502449
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Pro1039Leu
CA16043957
NM_001141974.3:c.3116C>T